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Passage Bio to Present at Chardan’s 7th Annual Genetic Medicines Conference

Key Takeaway: Passage Bio, Inc. announced that its CEO, William Chou, M.D., will participate in a fireside chat at Chardan's 7th Annual Genetic Medicines Conference on October 2, 2023. The company is focused on developing therapies for central nervous system disorders and has a portfolio addressing both pediatric and adult indications. With collaborations enhancing its capabilities, Passage Bio aims to advance their genetic medicines pipeline effectively.
Price reaction · baseline $13.502 (2023-09-22 close) · clean, no other PASG news in the window
day 0 close · peak
-0.8%

Market Sentiment Analysis

POSITIVE FACTORS

  • Participation in a significant industry conference highlights the company's commitment.
  • Focus on transformative therapies for CNS disorders with unmet needs.
  • Strong collaboration with the University of Pennsylvania enhances research capabilities.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Best trade, last catalyst
+26%
120-day peak, hindsight
Typical move
11.4%
average across 2 past catalysts
Cash runway
~8 mo
Medium dilution risk
Lead asset
PBFT02
Phase 1 · Frontotemporal Dementia

Full Press Release Details

PHILADELPHIA, Sept. 25, 2023 (GLOBE NEWSWIRE) -- Passage Bio, Inc. (NASDAQ: PASG), a clinical stage genetic medicines company focused on developing transformative therapies for central nervous system (CNS) disorders, today announced that William Chou, M.D., president and chief executive officer, will participate in a fireside chat at Chardan’s 7th Annual Genetic Medicines Conference on Monday, October 2, 2023 at 5:00 p.m ET.
A live webcast of the event will be available on the Investors & Media section of Passage Bio’s website at investors.passagebio.com. A replay of the presentation will be available for 30 days following the event.
Passage Bio (Nasdaq: PASG) is a clinical stage genetic medicines company on a mission to provide life-transforming therapies for patients with CNS diseases with limited or no approved treatment options. Our portfolio spans pediatric and adult CNS indications, and we are currently advancing clinical programs in GM1 gangliosidosis and frontotemporal dementia and our preclinical pipeline, including programs in amyotrophic lateral sclerosis and Huntington’s disease. Based in Philadelphia, PA, our company has established a strategic collaboration and licensing agreement with the renowned University of Pennsylvania’s Gene Therapy Program to conduct our discovery and IND-enabling preclinical work. Through this collaboration, we have enhanced access to a broad portfolio of gene therapy candidates and future gene therapy innovations that we then pair with our deep clinical, regulatory, manufacturing and commercial expertise to rapidly advance our robust pipeline of optimized gene therapies. As we work with speed and tenacity, we are always mindful of patients who may be able to benefit from our therapies. More information is available at www.passagebio.com.
For further information, please contact:
Passage Bio Investors:

Frequently Asked Questions

When is Passage Bio's fireside chat at the Genetic Medicines Conference?

The fireside chat will take place on October 2, 2023, at 5:00 p.m. ET.

Where can I watch the live webcast of the event?

The live webcast will be available on Passage Bio’s Investors & Media page.

What is the focus of Passage Bio's therapies?

Passage Bio develops therapies for central nervous system disorders with limited treatments.

Which CNS diseases are in Passage Bio's pipeline?

Their pipeline includes GM1 gangliosidosis, frontotemporal dementia, ALS, and Huntington’s disease.

Who is collaborating with Passage Bio for their research?

Passage Bio collaborates with the University of Pennsylvania’s Gene Therapy Program.

Last updated: Sep 25, 2023